A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872585



Internal ID22647525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:139963637..139963769hg38UCSC Ensembl
chrX:139045796..139045928hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436263
Samples
Known GenesCXorf66
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872585
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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